ENST00000307363.10:c.1998G=
MANE Select
|
ENSP00000306920.4:p.Pro666=
|
|
ENST00000307363.9:c.1998G=
|
ENSP00000306920.4:p.Pro666=
|
|
ENST00000307377.12:c.1605G=
|
ENSP00000305920.8:p.Pro535=
|
|
ENST00000399402.7:c.1908G=
|
ENSP00000382333.2:p.Pro636=
|
|
NM_000404.2:c.1998G=
|
NP_000395.2:p.Pro666=
|
|
NM_000404.3:c.1998G=
|
NP_000395.2:p.Pro666=
|
|
NM_001079811.1:c.1908G=
|
NP_001073279.1:p.Pro636=
|
|
NM_001079811.2:c.1908G=
|
NP_001073279.1:p.Pro636=
|
|
NM_001135602.1:c.1605G=
|
NP_001129074.1:p.Pro535=
|
|
NM_001135602.2:c.1605G=
|
NP_001129074.1:p.Pro535=
|
|
NM_001317040.1:c.2142G=
|
NP_001303969.1:p.Pro714=
|
|
NM_000404.4:c.1998G=
MANE Select
|
NP_000395.3:p.Pro666=
|
|
NM_001079811.3:c.1908G=
|
NP_001073279.2:p.Pro636=
|
|
NM_001135602.3:c.1605G=
|
NP_001129074.2:p.Pro535=
|
|
NM_001317040.2:c.2142G=
|
NP_001303969.2:p.Pro714=
|
|
NM_001393580.1:c.1734+16975G=
|
NP_001380509.1:n.1734+16975G=
|
|